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Anionic halogens /pseudohalogens

Addition of halogens and pseudohalogens to the cyclopropylthiocarbene chromium complexes 122 affords the 1,4-dihalo-1-phenylthio-l-alkenes 123 stereoselectively [65]. Electrophilic halogen is likely to activate the carbene complexes, followed by the homo-Michael addition of halide anion. (Scheme 44)... [Pg.126]

There are three important routes to the formation of the mercury-transition metal bond (a) displacement of halogen or pseudohalogen from mercury(II) salts with carbonyl metallate anions (b) reaction of a halo-phenylmercury compound with a transition metal hydride and (c) oxidative addition of a mercury halide to neutral zero valent metals.1 We report here the syntheses of three compounds containing three-centre, two-electron, mercury-ruthenium bonds utilizing trinuclear cluster anions and mercury(II) halides.2-4... [Pg.329]

HCo(CO)4are strong acids in aqueous solution. Both types of anions form precipitates with heavy metal ions such as Ag+ in aqueous solution. The parallels between seven-electron halogen atoms and 17-electron binary carbonyl species are sufficiently strong to justify applying the label pseudohalogen to these carbonyls.29... [Pg.97]

The halogen and pseudohalogen dimer radical anions, X2 (X = Cl, Br, I, SCN), react efficiently with phenols and phenolate ions to give the corresponding phenoxyl radicals (equation 6). [Pg.1110]

Another extension is Aat pseudohalogens can replace halogen, so that neutral and anionic isothiocyanates are also accessible by this method [5], as are heterometallic carbonyls [6]. A simple preparation of (Ph3PH)2CoCl4 makes a usefUl undergraduate laboratory experiment [2]. [Pg.22]

Pseudohalogen A linear or planar univalent radical that, like the halogens, can form anions, salts, and covalent derivatives. [Pg.160]

Gulaboski, R., K. Riedl, and R Scholz, Standard Gibbs energies of transfer of halo-genate and pseudohalogenate ions, halogen substituted acetates, and cycloalkyl car-boxylate anions at the water I nitrobenzene interface, Phys Chem Chem Phys, Vol. 5, (2003) p. 1284. [Pg.101]


See other pages where Anionic halogens /pseudohalogens is mentioned: [Pg.336]    [Pg.337]    [Pg.284]    [Pg.776]    [Pg.333]    [Pg.440]    [Pg.656]    [Pg.657]    [Pg.22]    [Pg.438]    [Pg.440]    [Pg.61]    [Pg.446]    [Pg.26]    [Pg.438]    [Pg.557]    [Pg.427]    [Pg.398]    [Pg.852]    [Pg.273]    [Pg.580]    [Pg.174]    [Pg.34]    [Pg.852]    [Pg.445]    [Pg.621]    [Pg.668]    [Pg.66]    [Pg.147]   
See also in sourсe #XX -- [ Pg.22 ]




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Pseudohalogen

Pseudohalogens

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